Defining the transmissible dose 50% for two pandemic influenza viruses in ferrets.

IF 3.8 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2026-04-21 Epub Date: 2026-03-11 DOI:10.1128/jvi.01635-25
C J Field, K M Septer, D R Patel, V C Weaver, D G Sim, K H Restori, M F Boni, T C Sutton
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Abstract

Ferrets are widely used to model airborne transmission of influenza viruses in humans. Airborne transmission is evaluated by infecting donor ferrets with a high virus dose and monitoring transmission to contact animals sharing the same airspace. Humans can be infected with a broad range of influenza virus doses. Therefore, we evaluated the relationship between inoculation dose and transmission for two pandemic influenza viruses in ferrets. Donor ferrets were inoculated with 100 to 106 tissue culture infectious dose 50 (TCID50) of the 2009 pandemic H1N1 or 1968 pandemic H3N2 virus and were then paired with respiratory contacts. Using the proportion of donors that became infected across virus doses, we calculated the infectious dose 50 (ID50). Subsequently, by comparing the proportion of contacts that became infected, we calculated the transmissible dose 50% (TD50): the donor inoculation dose that resulted in transmission to 50% of contacts. For the 2009 pandemic H1N1 virus, the ID50 and TD50 were equivalent at <1 TCID50. However, for the 1968 pandemic H3N2 virus, the ID50 and TD50 were 100.5 and 104.08 TCID50 (95% CI: 102.34-105.82), respectively. The increased TD50 for the H3N2 virus was associated with significant reductions in peak viral titers and viral shedding in donors over decreasing virus inoculation doses. Collectively, these studies define a new measure of transmission that permits comparisons of transmissibility between viral strains and subtypes in ferrets. We show that the 1968 pandemic H3N2 virus has a higher TD50 and reduced transmissibility in ferrets relative to the 2009 pandemic H1N1 virus.

Importance: Ferrets are the gold standard animal model used to assess the transmissibility of influenza viruses. Airborne transmission is evaluated by infecting donor ferrets with a high virus dose and monitoring transmission to contact animals sharing the same airspace. However, the relationship between inoculation dose and transmission has not been evaluated in ferrets. Therefore, we performed studies evaluating airborne transmission of the 2009 pandemic H1N1 and 1968 pandemic H3N2 viruses over log scale reductions in donor inoculation doses. Using the results of these studies, we define a new measure of transmission, the transmissible dose 50%: the donor inoculation dose at which a virus is transmitted to 50% of contacts. Importantly, this metric permits the evaluation of transmissibility over a log scale. We demonstrate that the 1968 pandemic H3N2 virus has reduced transmissibility compared to the 2009 pandemic H1N1 virus in ferrets.

确定两种大流行性流感病毒在雪貂中的传播剂量为50%。
雪貂被广泛用于模拟流感病毒在人类中的空气传播。通过用高病毒剂量感染供体雪貂并监测传播到共享同一空域的接触动物来评估空气传播。人类可感染多种剂量的流感病毒。因此,我们评估了接种剂量与两种大流行性流感病毒在雪貂中的传播之间的关系。将2009年H1N1或1968年H3N2大流行病毒的组织培养感染剂量50 (TCID50)接种给供体雪貂,接种剂量为100 ~ 106,然后与呼吸道接触者配对。利用不同病毒剂量的供体感染比例,我们计算了感染剂量50 (ID50)。随后,通过比较接触者感染的比例,我们计算了50%的传播剂量(TD50):供体接种剂量导致50%的接触者传播。对于2009年H1N1大流行病毒,ID50和TD50在50是相等的。然而,1968年大流行H3N2病毒的ID50和TD50分别为100.5和104.08 TCID50 (95% CI: 102.34-105.82)。H3N2病毒TD50的增加与供体病毒峰值滴度的显著降低和病毒脱落有关。总的来说,这些研究定义了一种新的传播方法,可以比较病毒株和亚型在雪貂中的传播性。我们发现1968年大流行的H3N2病毒相对于2009年大流行的H1N1病毒具有更高的TD50和较低的雪貂传播性。重要性:雪貂是用于评估流感病毒传播性的金标准动物模型。通过用高病毒剂量感染供体雪貂并监测传播到共享同一空域的接触动物来评估空气传播。然而,在雪貂中,接种剂量与传播之间的关系尚未得到评估。因此,我们进行了研究,评估2009年H1N1大流行和1968年H3N2大流行病毒在供体接种剂量对数尺度减少后的空气传播。利用这些研究的结果,我们定义了一种新的传播度量,即50%的传播剂量:供体接种剂量,在该剂量下病毒传播给50%的接触者。重要的是,该度量允许在对数尺度上评估传递率。我们证明1968年大流行的H3N2病毒与2009年大流行的H1N1病毒相比,在雪貂中的传播性降低了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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